Issue 0, 1982

Photo-oxidation of oxazolidones and hydantoins in the presence of benzophenone

Abstract

Irradiation in the presence of benzophenone and oxygen of nitrogen-containing heterocycles having an NCO group yields products arising out of regioselective oxidation α to the nitrogen atom. Direct irradiation (in the absence of benzophenone and oxygen) of 5-methyl- and 5,5-dimethyl-hydantoins yields allophanates. The first step of this reaction involves the homolysis of the C(4)–C(5) bond of the hydantoin.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1982, 2341-2345

Photo-oxidation of oxazolidones and hydantoins in the presence of benzophenone

J. Gramain and R. Remuson, J. Chem. Soc., Perkin Trans. 1, 1982, 2341 DOI: 10.1039/P19820002341

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